Synthesis of bis(amino)furans from biomass based 5-hydroxymethyl furfural
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摘要:
In this study we report a new reaction pathway in which the hydroxyl and the aldehyde groups of 5-hydroxymethyl furfural were aminated respectively.Hydroxyl group was aminated via Ritter reaction followed by direct reductive amination of aldehyde group.For the Ritter reaction of 5-hydroxymethyl furfural,mixture of trifluoromethane sulfonic acid and phosphoric anhydride showed good performance and the intermediate N-acyl-5-aminomethyl furfural with the highest yield of 89.1 wt% was obtained.Optimization of direct reductive amination of 2,5-bis(aminomethyl) furan was conducted and a yield of 45.7 wt% was achieved.This study presents a simple way for preparing bis(amino)furans from renewable biomass based 5-hydroxymethyl furfural,which enriches the biorefinery concept from biomass.